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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 40033Generated: October 26, 2026

2-Methyl-2-butene → 1-Benzyl-2-isopropyl-6-methoxy-1H-indole-3-carboxylic Acid

https://huagongshe.com/reaction/40033

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methyl-2-buteneHCID 10553—
ReactantMonobasic potassium phosphateHCID 516951—
ReactantSodium ChloriteHCID 23668197—
Reactant1-Benzyl-2-isopropyl-6-methoxy-1H-indole-3-carbaldehydeHCID 59762394—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Solventtert-ButanolHCID 6386—
Product1-Benzyl-2-isopropyl-6-methoxy-1H-indole-3-carboxylic AcidHCID 59762354—

Reaction Steps

To a solution of 1-benzyl-2-isopropyl-6-methoxy-1H-indole-3-carbaldehyde (Compound 5, 608 mg, 1.98 mmol) in t-BuOH (15 ml), CH3CN (15 ml), and 2-methyl-2-butene (10 ml) was added a solution of KH2PO4 (5.4 g, 39.6 mmol) and NaClO2 (80%, 4.5 g, 39.6 mmol) in H2O (50 ml). The mixture was stirred at room temperature and additional 2-methyl-2-butene, KH2PO4, and NaClO2 were added at the above ratio every 16-24 h until the starting material was consumed. The reaction mixture was extracted with EtOAc (×3) and the combined organic layer was washed with brine, dried over Na2SO4, and concentrated in vacuo. The residue was purified by chromatography on silica gel (0→25% EtOAc-hexanes) to yield the title compound as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524917B2
Source datasetuspto-grants-2013_09
ORD IDord-df34ff595be44ca7a2a241a02c99ab6e
Source noteuspto-grants-2013_09